Canonical Allele Identifier: CA2427976125
Gene: SYN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47588547A= , CM000685.2:g.47588547A= GRCh38
NC_000023.10:g.47447946A= , CM000685.1:g.47447946A= GRCh37
NC_000023.9:g.47332890A= NCBI36
NG_008437.1:g.36311T=
NG_012533.1:g.11257A=

Transcript Alleles

HGVS Amino-acid change
ENST00000295987.13:c.775-11046T= MANE Select ENSP00000295987.7:n.775-11046T=
ENST00000340666.5:c.775-11046T= ENSP00000343206.4:n.775-11046T=
ENST00000295987.11:c.775-11046T= ENSP00000295987.7:n.775-11046T=
ENST00000340666.4:c.775-11046T= ENSP00000343206.4:n.775-11046T=
NM_006950.3:c.775-11046T= MANE Select NP_008881.2:n.775-11046T=
NM_133499.2:c.775-11046T= NP_598006.1:n.775-11046T=
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